Product Details

SNP ID
rs201299613
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:1403273 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATGAACATGCTGCCTGGGCTTCAG[C/G]GGGCCACTTTGGTGGCCAAGATGGC
Phenotype
MIM: 300162 MIM: 400011
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
ASMTL PubMed Links

Gene Details

Gene
ASMTL
Gene Name
acetylserotonin O-methyltransferase-like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001173473.1 1914 Missense Mutation CCC,CGC P563R NP_001166944.1
NM_001173474.1 1914 Missense Mutation CCC,CGC P605R NP_001166945.1
NM_004192.3 1914 Missense Mutation CCC,CGC P621R NP_004183.2
XM_005274434.3 1914 Missense Mutation CCC,CGC P621R XP_005274491.1
XM_011546185.2 1914 Missense Mutation CCC,CGC P538R XP_011544487.1
XM_017029919.1 1914 Missense Mutation CCC,CGC P512R XP_016885408.1

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